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並前往https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K023574

510(k) Premarket Notification - FDA

Device Classification Name, wheelchair, mechanical 22. 510(k) Number, K023574. Device Name, GIZMO. Applicant. FREEDOM DESIGNS, INC. 2241 MADERA RD.

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